blastp_kegg |
lcl|pmum:103325809
|
1 |
247 |
+ |
247 |
Gaps:2 |
47.98 |
519 |
64.26 |
5e-114 |
cytochrome P450 CYP72A219-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa004271mg
|
17 |
247 |
+ |
231 |
none |
44.51 |
519 |
66.23 |
1e-112 |
hypothetical protein
|
blastp_kegg |
lcl|pper:PRUPE_ppa016770mg
|
17 |
247 |
+ |
231 |
none |
45.65 |
506 |
66.23 |
2e-111 |
hypothetical protein
|
blastp_kegg |
lcl|pmum:103325808
|
1 |
245 |
+ |
245 |
Gaps:2 |
47.59 |
519 |
62.75 |
1e-110 |
cytochrome P450 CYP72A219-like
|
blastp_kegg |
lcl|cit:102610281
|
1 |
247 |
+ |
247 |
none |
47.78 |
517 |
60.32 |
2e-108 |
11-oxo-beta-amyrin 30-oxidase-like
|
blastp_kegg |
lcl|pxb:103931558
|
21 |
247 |
+ |
227 |
none |
43.74 |
519 |
63.88 |
8e-107 |
cytochrome P450 CYP72A219-like
|
blastp_kegg |
lcl|cit:102609394
|
1 |
247 |
+ |
247 |
none |
93.92 |
263 |
59.11 |
1e-106 |
secologanin synthase-like
|
blastp_kegg |
lcl|fve:101311035
|
1 |
247 |
+ |
247 |
none |
45.49 |
543 |
59.11 |
2e-106 |
secologanin synthase-like
|
blastp_kegg |
lcl|mdm:103448666
|
1 |
247 |
+ |
247 |
Gaps:2 |
47.98 |
519 |
61.04 |
1e-105 |
cytochrome P450 CYP72A219-like
|
blastp_kegg |
lcl|vvi:100260702
|
3 |
247 |
+ |
245 |
none |
47.57 |
515 |
60.41 |
2e-105 |
secologanin synthase-like
|
blastp_uniprot_sprot |
sp|H1A988|C7254_GLYUR
|
8 |
231 |
+ |
224 |
Gaps:4 |
43.21 |
523 |
55.75 |
5e-80 |
11-oxo-beta-amyrin 30-oxidase OS Glycyrrhiza uralensis GN CYP72A154 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q05047|C72A1_CATRO
|
1 |
245 |
+ |
245 |
Gaps:5 |
47.71 |
524 |
45.60 |
1e-75 |
Secologanin synthase OS Catharanthus roseus GN CYP72A1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|H1A981|C7263_MEDTR
|
8 |
235 |
+ |
228 |
Gaps:4 |
44.27 |
524 |
50.00 |
1e-72 |
11-oxo-beta-amyrin 30-oxidase OS Medicago truncatula GN CYP72A63 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9SHG5|C72C1_ARATH
|
3 |
245 |
+ |
243 |
none |
46.82 |
519 |
42.80 |
4e-71 |
Cytochrome P450 72C1 OS Arabidopsis thaliana GN CYP72C1 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|O48786|C734A_ARATH
|
12 |
247 |
+ |
236 |
Gaps:1 |
45.58 |
520 |
40.51 |
2e-59 |
Cytochrome P450 734A1 OS Arabidopsis thaliana GN CYP734A1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|B9X287|C7346_ORYSJ
|
24 |
247 |
+ |
224 |
Gaps:7 |
42.62 |
542 |
33.77 |
1e-45 |
Cytochrome P450 734A6 OS Oryza sativa subsp. japonica GN CYP734A6 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q8LIF2|C7345_ORYSJ
|
28 |
247 |
+ |
220 |
Gaps:7 |
42.27 |
537 |
33.48 |
7e-38 |
Cytochrome P450 734A5 OS Oryza sativa subsp. japonica GN CYP734A5 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q6Z6D6|C7342_ORYSJ
|
28 |
247 |
+ |
220 |
Gaps:6 |
40.57 |
557 |
30.97 |
2e-37 |
Cytochrome P450 734A2 OS Oryza sativa subsp. japonica GN CYP734A2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q69XM6|C7344_ORYSJ
|
24 |
247 |
+ |
224 |
Gaps:5 |
42.57 |
538 |
29.69 |
7e-37 |
Cytochrome P450 734A4 OS Oryza sativa subsp. japonica GN CYP734A4 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q2QYH7|C14C2_ORYSJ
|
12 |
244 |
+ |
233 |
Gaps:20 |
47.32 |
522 |
29.96 |
1e-24 |
Cytochrome P450 714C2 OS Oryza sativa subsp. japonica GN CYP714C2 PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|177927
|
8 |
247 |
+ |
240 |
Gaps:22 |
47.67 |
516 |
31.30 |
8e-28 |
PLN02290 PLN02290 cytokinin trans-hydroxylase.
|
rpsblast_cdd |
gnl|CDD|200971
|
99 |
217 |
+ |
119 |
Gaps:12 |
26.68 |
461 |
23.58 |
8e-13 |
pfam00067 p450 Cytochrome P450. Cytochrome P450s are haem-thiolate proteins involved in the oxidative degradation of various compounds. They are particularly well known for their role in the degradation of environmental toxins and mutagens. They can be divided into 4 classes according to the method by which electrons from NAD(P)H are delivered to the catalytic site. Sequence conservation is relatively low within the family - there are only 3 absolutely conserved residues - but their general topography and structural fold are highly conserved. The conserved core is composed of a coil termed the 'meander' a four-helix bundle helices J and K and two sets of beta-sheets. These constitute the haem-binding loop (with an absolutely conserved cysteine that serves as the 5th ligand for the haem iron) the proton-transfer groove and the absolutely conserved EXXR motif in helix K. While prokaryotic P450s are soluble proteins most eukaryotic P450s are associated with microsomal membranes. their general enzymatic function is to catalyze regiospecific and stereospecific oxidation of non-activated hydrocarbons at physiological temperatures.
|
rpsblast_kog |
gnl|CDD|35379
|
1 |
245 |
+ |
245 |
Gaps:31 |
45.07 |
497 |
27.23 |
3e-28 |
KOG0157 KOG0157 KOG0157 Cytochrome P450 CYP4/CYP19/CYP26 subfamilies [Secondary metabolites biosynthesis transport and catabolism Lipid transport and metabolism].
|
rpsblast_kog |
gnl|CDD|35380
|
91 |
243 |
+ |
153 |
Gaps:14 |
31.86 |
499 |
23.27 |
1e-12 |
KOG0158 KOG0158 KOG0158 Cytochrome P450 CYP3/CYP5/CYP6/CYP9 subfamilies [Secondary metabolites biosynthesis transport and catabolism].
|
rpsblast_kog |
gnl|CDD|35378
|
90 |
247 |
+ |
158 |
Gaps:15 |
34.15 |
489 |
22.75 |
3e-10 |
KOG0156 KOG0156 KOG0156 Cytochrome P450 CYP2 subfamily [Secondary metabolites biosynthesis transport and catabolism].
|